EP0095233A2 - Procédé de préparation d'un polymère de monoallylamine - Google Patents

Procédé de préparation d'un polymère de monoallylamine Download PDF

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Publication number
EP0095233A2
EP0095233A2 EP83301719A EP83301719A EP0095233A2 EP 0095233 A2 EP0095233 A2 EP 0095233A2 EP 83301719 A EP83301719 A EP 83301719A EP 83301719 A EP83301719 A EP 83301719A EP 0095233 A2 EP0095233 A2 EP 0095233A2
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EP
European Patent Office
Prior art keywords
group
monoallylamine
polymerization
azo
nitrogen atom
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Granted
Application number
EP83301719A
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German (de)
English (en)
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EP0095233A3 (en
EP0095233B1 (fr
Inventor
Susumu Harada
Sakuro Hasegawa
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Nitto Boseki Co Ltd
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Nitto Boseki Co Ltd
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Publication of EP0095233A3 publication Critical patent/EP0095233A3/en
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
    • C08F22/02—Acids; Metal salts or ammonium salts thereof, e.g. maleic acid or itaconic acid
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F26/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
    • C08F26/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen

Definitions

  • allyl compounds are difficult to be polymerized with usual radical initiators and they only,give a polymer having a low degree of polymerization in a low yield.
  • monoallylamine which is a kind of allyl compound.
  • monoallylamine hardly polymerizes with radical or ionic initiators, and only a few examples of polymerization have been reported in which the polymerization takes place under the following special conditions.
  • the above-mentioned processes 1, 2 and 3 are examples of polymerization of monoallylamine in which catalysts such as radical initiators are used.
  • the processes 1 and 2 the polymers obtained are viscous and resinous and no polymer having a high degree of polymerization is obtained.
  • the process 3 disclosed in the German Laid-Open Gazette relates to homo- and copolymerization of monoallylamine hydrochloride.
  • all working examples except one mentioned at page 36 thereof are those of copolymerizing monoallylamine hydrochloride with a polymerizable vinyl monomer such as acrylamide, acrylic acid, acrylic acid ester and acrylonitrile.
  • polymerizable vinyl monomer such as acrylamide, acrylic acid, acrylic acid ester and acrylonitrile.
  • polyallylamine hydrochloride was obtained at a yield of 85%.
  • German Laid-Open Gazette does not mention the properties and the polymerization degree of the polymer obtained but only discribes that it is water-soluble over the whole pH range.
  • the following radiation polymerization processes have also been proposed as processes for polymerizing monoallylamine.
  • the monoallylamine polymers obtained by these processes have a higher degree of polymerization than that of the polymers obtained by the processes using radical type catalysts.
  • the radiation polymerization processes with gamma rays in protic solvents mentioned in (4) and (5) are relatively preferable.
  • radiation polymerization process is not excellent as a process for producing a large amount of polymer, and at the present stage there is no case of industrially producing a polymer by radiation polymerization process.
  • polyallylamine is not produced industrially even today, whereas monoallylamine has been industrially produced from many years ago.
  • An object of this invention is to provide an industrially excellent process for polymerizing mono- allyalmine by using a radical initiator.
  • Another object of this invention is to provide a process for producing a polymer of monoallylamine, having a high degree of polymerization, by using a radical initiator.
  • the present inventors have searched for a process for producing a polymer having a high degree of polymerization in a high yield by radical-polymerizing monoallylamine under industrially readily practicable conditions. As the result, they have discovered a surprising fact that, if a radical initiator having an azo group and a group having cationic nitrogen atom in its molecule is used, an inorganic acid salt of monoallylamine can be polymerized in a polar solvent quite easily and thereby a polymer having a high degree of polymerization can be obtained in a high yield.
  • this invention consists in a process for producing a polymer of monoallylamine which comprises polymerizing an inorganic acid salt of monoallylamine in a polar solvent in the presence of a radical initiator having an azo group and a group having cationic nitrogen atom in its molecule.
  • hydrochloric acid salt sulfuric acid salt, sulfurous acid salt, phosphoric acid salt and the like can be referred to.
  • the polymerization is carried out in a polar solvent, of which examples include water, inorganic acids (hydrochloric acid, sulfuric acid, phosphoric acid and polyphosphoric acid) or their aqueous solutions, organic acids (formic acid, acetic acid, propionic acid, lactic acid and the like) or their aqueous solutions, alcohols, dimethyl sulfoxide, dimethylformamide, and aqueous solutions of inorganic acid salts (zinc chloride, calcium chloride, magnesium chloride and the like).
  • a polar solvent of which examples include water, inorganic acids (hydrochloric acid, sulfuric acid, phosphoric acid and polyphosphoric acid) or their aqueous solutions, organic acids (formic acid, acetic acid, propionic acid, lactic acid and the like) or their aqueous solutions, alcohols, dimethyl sulfoxide, dimethylformamide, and aqueous solutions of inorganic acid salts (zinc chloride, calcium chloride, magnesium chloride and the like
  • the above-mentioned inorganic acid salts of allylamine are usually employed in the form of an isolated crystal. However, it is also allowable to form the salt in situ by adding monoallylamine and inorganic acid into the above-mentioned polar solvent. It is needless to say that, when an.inorganic acid or its aqueous solution is used as the medium of polymerization, a predetermined quantity of monoallylamine may be added to the acid or its aqueous solution and then it may be polymerized directly.
  • the initiator used in this invention is a radical initiator having an azo group and a group having cationic nitrogen atom in its molecule.
  • inorganic or organic acid salts of azo compounds including hydrochloride, sulfate, phosphate, alkyl- sulfate, paratoluene sulfonate, formate, acetate and propionate and said azo compounds being represented by the following general formula [I] : [wherein at least one, preferably both of R 1 and R 2 is a group having cationizable nitrogen atom selected from the group consisting of aminoalkyl, aminoaryl, amidinylalkyl, amidinylaryl, aminoalkaryl, aminoaralkyl, amidinylaralkyl, amidinylalkaryl, cyanoaminoalkyl and cyanoaminoalkaryl.
  • R 1 and R 2 are said group having cationizable nitrogen atom, the other is a group selected from the group consisting of alkyl, aryl, alkaryl, aralkyl, cyanoalkyl, cyanoaryl, cyanoalkaryl and cyanoaralkyl.
  • R1 and R 2 taken together, may form a single alkylene group represented by the following general formula (II): (wherein R is a group selected from the group consisting of alkylene, alkylalkylene and arylalkylene, covalent bonds (a) and (b) link with the respective nitrogen atoms of azo group to form an azo group-containing ring, and X' is a group having cationizable nitrogen atom.)]
  • initiators represented by general formula (I) particularly preferable are the compounds having secondary or tertiary carbon atom adjacent to azo group, of which typical examples are as follows:
  • radical initiators having an azo group and a group having cationic nitrogen atom are known compounds, and the processes for producing them and examples of polymerization of unsaturated compounds using them as initiator are disclosed in US Patent Nos. 2,599,299, 2,599,300, 2,605,260 and 2,744,105.
  • ethylene, acrylonitrile, chlorobutadiene or the like is used as the unsaturated compound to be polymerized, and these unsaturated compounds are different from monoallylamine in chemical structure and properties. Therefore, these US patents do not suggest that monoallylamine can be polymerized similarly.
  • the amount of the initiator used in this invention is 0.1-10% by weight and usually 1-6% by weight, based on the weight of inorganic acid salt of monoallylamine.
  • the temperature of polymerization varies depending on the chemical structure of initiator, it is 30° - 100°C and usually 40° - 70°C.
  • the time period of polymerization is usually 100 hours or less.
  • concentration of the starting monomer a higher concentration is more desirable in the scope of its solubility. Usually it is in the range of 10 to 85% by weight.
  • the polymerization is retarded by oxygen in the air to some extent, it is preferably carried out in an inert gas such as nitrogen.
  • radical initiators other than the radical initiators used in this invention have an ability to polymerize inorganic acid salt of monoallylamine in polar solvent to some extent.
  • MAA monoallylamine
  • Shell Chemical Co. USA was used as starting monomer. It was dried on granular caustic soda and rectified under a stream of nitrogen, and a fraction having a boiling point of 52.5-53°C was used for the polymerization. By gas chromatography, it was revealed that this fraction contained neither diallylamine nor triallylamine at all.
  • MAA-HC1 polyallyalmine hydrochloride by the polymerization of MAA hydrochloride
  • azo initiator-1 2,2'- bis(N-phenylamidinyl)-2,2'-azopropane dihydrochloride
  • Initiator-1 2,2'- bis(N-phenylamidinyl)-2,2'-azopropane dihydrochloride
  • this PAA-HCl As determined by the measurement of osmotic pressure in aqueous solution of sodium chloride, this PAA-HCl has a number-average molecular weight (M ) of 8,500 (number-average degree of polymerization: 91).
  • This PAA-HCl was readily soluble in water and aqueous acids, and was insoluble in organic solvents. Its aqueous solution exhibited a typical viscosity behavior of polyelectrolyte.
  • PAA free polyallylamine
  • 30 g of PAA-HCl was dissolved into 270 g of distilled water and passed through strongly basic ion exchange resin (Amberlite IRA-402) to remove the hydrochloric acid, after which the filtrate was freeze-dried to obtain 16.5 g of white-colored PAA.
  • This PAA was readily soluble in water and methanol, swellable in dimethyl sulfoxide and pyridine and insoluble in other usual organic solvents. When allowed to stand in the air, this PAA absorbed carbon dioxide and water to form a carbonate.
  • Example 2 Using 2,2'-diamidinyl-2,2'-azopropane dihydrochloride (Initiator-2) in place of Initiator-l used in Example 1, polymerization was carried out by the same procedure as in Example 1, provided that an aqueous solution obtained by dissolving 14 g of Initiator-2 into 30 ml of distilled water was added not at once at the start of polymerization but in two portions, firstly at the start of polymerization and secondly 30 hours after it. Subsequently, the reaction mixture was treated in the same manner as in Example 1 to obtain 503 g (85%) of PAA-HC1. M of this polymer was 7,500.
  • Example 2 Into the 2 liter polymerization vessel used in Example 1 equipped with a dropping.funnel in place of the nitrogen inlet tube was introduced 613 g (5 moles) of 80% sulfuric acid, into which was dropped 2.85 g (5 moles) of MAA while cooling and stirring the sulfuric acid. After dropping it, the mixture was heated to 50°C to obtain a homogeneous solution. To this solution was added a solution obtained by dissolving 8.6 g of Initiator-1 into 20 ml of distilled water. Subsequently, polymerization was carried out for 48 hours while keeping the mixture at 50 ⁇ 2°C.
  • the resulting colorless, transparent, viscous solution was thrown into a large amount of water, whereby the polymer precipitated in the form of a paste.
  • the precipitate was dissolved into 900 ml of concentrated hydrochloric acid, and the resulting solution was thrown into a large amount of methanol to precipitate it as PAA-HCl.
  • the precipitate was collected by filtration, dried, again dissolved into 500 ml of concentrated hydrochloric acid and reprecipitated by throwing it into methanol.
  • the precipitate was collected by filtration and extracted by means of Soxhlet extractor to remove the unpolymerized monomer and sulfuric acid.
  • the precipitate was dried under reduced pressure at 50°C to obtain 440 g (yield about 90%) of PAA-HC1. M of this polymer was 6,500.
  • Example 2 Into the 2 liter polymerization vessel used in Example 1 equipped with a dropping funnel in place of the nitrogen gas inlet tube was dropped 1,150 g (10 moles) of 85% phosphoric acid, into which was dropped 285 g (5 moles) of MAA with stirring. At this time, the temperature was kept at 10 - 30°C. If the temperature exceeds 30°C, MAA can vaporize partially. If the temperature is lower than 10°C, phosphate of MAA deposite out as a crystal, which is inconvenient.
  • MAA inorganic acid salts were subjected to polymerization treatment in various solvents by using, as catalyst, various radical initiators other than the radical initiators of this invention (Comparative Examples 1 - 9).
  • MAA not formed into inorganic acid salt, was directly subjected to polymerization treatment in the presence of the initiator used in this invention (Comparative Example 10).
  • allyl alcohol which is other allyl compound, was subjected to polymerization treatment in the presence of the initiator used in this invention (Comparative Example 11). All these polymerization treatments were carried out in a stoppered 50 ml test tube in an atmosphere of nitrogen by the procedure of standing polymerization. After the polymerization treatment, the polymer was separated and purified by the procedure mentioned in the preceding examples, provided that the extraction by means of Soxhlet extractor was not carried out. The results are summarized in the following Table 2.
  • the reaction mixture was cooled to 20°C, filtered off, washed with ethylacetate and dried at 60°C in vacuo to obtain 0.25 g (yield 0.53%) of yellowish hygroscopic solid product; Since the product was obtained in a small amount, it was impossible to determine the degree of polymerization thereof. However the hygroscopic character of the product means that it has a relatively low degree of polymerization.
  • the process of this invention obviously has a superiority to the conventionally employed radical polymerization processes.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polymerization Catalysts (AREA)
  • Polymerisation Methods In General (AREA)
EP83301719A 1982-05-19 1983-03-28 Procédé de préparation d'un polymère de monoallylamine Expired EP0095233B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US379983 1982-05-19
US06/379,983 US4504640A (en) 1982-05-19 1982-05-19 Process for producing monoallylamine polymer

Publications (3)

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EP0095233A2 true EP0095233A2 (fr) 1983-11-30
EP0095233A3 EP0095233A3 (en) 1984-03-21
EP0095233B1 EP0095233B1 (fr) 1986-06-04

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US (1) US4504640A (fr)
EP (1) EP0095233B1 (fr)
JP (1) JPS58201811A (fr)
KR (1) KR890002931B1 (fr)
AU (1) AU539800B2 (fr)
CA (1) CA1233945A (fr)
DE (1) DE3363895D1 (fr)

Cited By (19)

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EP0140309A2 (fr) * 1983-10-21 1985-05-08 Nitto Boseki Co., Ltd. Procédé de préparation de copolymères de monoallylamines et de derivés de diallylamine
EP0145220A2 (fr) * 1983-11-10 1985-06-19 Nitto Boseki Co., Ltd. Procédé de production de polymères de monoallylamine
US4540760A (en) * 1984-01-11 1985-09-10 Nitto Boseki Co. Ltd. Process for producing polymers of monoallylamine
EP0173963A2 (fr) * 1984-09-01 1986-03-12 Nitto Boseki Co., Ltd. Polymères de monoallylamines secondaires n-substitués et leurs sels et procédé de leur préparation
EP0190704A1 (fr) * 1985-02-04 1986-08-13 Nitto Boseki Co., Ltd. Procédé de préparation de polymères de sels d'acides inorganiques de monoallylamines ou de monoallylamines N-substituées
US4614593A (en) * 1985-03-28 1986-09-30 Ethyl Corporation Demulsification of oil-in-water emulsions
EP0196588A2 (fr) * 1985-03-29 1986-10-08 Nitto Boseki Co., Ltd. Procédé de préparation de copolymères de monoallylamines secondaires N-substituées et leurs sels
US4657948A (en) * 1985-05-09 1987-04-14 Ethyl Corporation Fluid loss control in well cement slurries
US4661263A (en) * 1985-02-19 1987-04-28 Ethyl Corporation Water clarification
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US5028675A (en) * 1986-04-30 1991-07-02 Southwest Foundation For Biomedical Research Polyamide resin and method for preparation of reagents for immunodiagnostic use
EP0131306B1 (fr) * 1983-07-11 1993-09-29 Nitto Boseki Co., Ltd. Agent améliorant l'égouttage d'une suspension de pâte
US5296572A (en) * 1986-04-30 1994-03-22 James Sparrow Large pore polyamide resin and method of preparation thereof
EP2597123A1 (fr) 2011-11-23 2013-05-29 Basf Se Liant aqueux pour substrats granuleux et/ou fibreux
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JPS60106850A (ja) * 1983-11-14 1985-06-12 Nitto Boseki Co Ltd ポリアリルアミン重合体溶液の調製方法
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CA2330663C (fr) * 1999-03-03 2007-07-31 Nitto Boseki Co., Ltd. Procede de fabrication d'une solution aqueuse d'un polymere monoallylamine
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US8251503B2 (en) 2008-04-04 2012-08-28 Konica Minolta Ij Technologies, Inc. Nonaqueous ink jet ink, process for producing nonaqueous ink jet ink, and ink jet recording method
US8389640B2 (en) * 2008-04-15 2013-03-05 Lupin Limited Process for the preparation of cross-linked polyallylamine polymer
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Cited By (26)

* Cited by examiner, † Cited by third party
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EP0131306B1 (fr) * 1983-07-11 1993-09-29 Nitto Boseki Co., Ltd. Agent améliorant l'égouttage d'une suspension de pâte
EP0140309A2 (fr) * 1983-10-21 1985-05-08 Nitto Boseki Co., Ltd. Procédé de préparation de copolymères de monoallylamines et de derivés de diallylamine
EP0140309A3 (en) * 1983-10-21 1985-10-30 Nitto Boseki Co., Ltd. Process for the preparation of copolymers of monoallylamine and diallylamine derivatives
EP0145220A2 (fr) * 1983-11-10 1985-06-19 Nitto Boseki Co., Ltd. Procédé de production de polymères de monoallylamine
EP0145220A3 (en) * 1983-11-10 1985-10-23 Nitto Boseki Co., Ltd. Process for producing polymers of monoallylamine
US4540760A (en) * 1984-01-11 1985-09-10 Nitto Boseki Co. Ltd. Process for producing polymers of monoallylamine
EP0173963A2 (fr) * 1984-09-01 1986-03-12 Nitto Boseki Co., Ltd. Polymères de monoallylamines secondaires n-substitués et leurs sels et procédé de leur préparation
EP0173963A3 (fr) * 1984-09-01 1986-08-13 Nitto Boseki Co., Ltd. Polymères de monoallylamines secondaires n-substitués et leurs sels et procédé de leur préparation
US4644042A (en) * 1984-09-01 1987-02-17 Nitto Boseki Co., Ltd. Polymers of N-substituted secondary monoallylamines and their salts and process for producing the same
EP0190704A1 (fr) * 1985-02-04 1986-08-13 Nitto Boseki Co., Ltd. Procédé de préparation de polymères de sels d'acides inorganiques de monoallylamines ou de monoallylamines N-substituées
US4661263A (en) * 1985-02-19 1987-04-28 Ethyl Corporation Water clarification
US4614593A (en) * 1985-03-28 1986-09-30 Ethyl Corporation Demulsification of oil-in-water emulsions
EP0196588A3 (fr) * 1985-03-29 1987-04-22 Nitto Boseki Co., Ltd. Procédé de préparation de copolymères de monoallylamines secondaires N-substituées et leurs sels
EP0196588A2 (fr) * 1985-03-29 1986-10-08 Nitto Boseki Co., Ltd. Procédé de préparation de copolymères de monoallylamines secondaires N-substituées et leurs sels
US4706755A (en) * 1985-05-09 1987-11-17 Ethyl Corporation Fluid loss control in well cement slurries
US4657948A (en) * 1985-05-09 1987-04-14 Ethyl Corporation Fluid loss control in well cement slurries
US4698380A (en) * 1985-09-23 1987-10-06 Ethyl Corporation Fluid loss control in well cement slurries
US4927896A (en) * 1986-04-25 1990-05-22 Ethyl Corporation Process for polymerizing monoallylamine
US5296572A (en) * 1986-04-30 1994-03-22 James Sparrow Large pore polyamide resin and method of preparation thereof
US5028675A (en) * 1986-04-30 1991-07-02 Southwest Foundation For Biomedical Research Polyamide resin and method for preparation of reagents for immunodiagnostic use
US5512648A (en) * 1986-04-30 1996-04-30 James Sparrow Polyamide resin-protide conjugate, preparation and uses
FR2601022A1 (fr) * 1986-07-02 1988-01-08 Sandoz Sa Homopolymeres de la diallylamine et de ses derives, leur preparation et leur utilisation dans le traitement des textiles
CH677857GA3 (fr) * 1986-07-02 1991-07-15
US8512618B2 (en) 2007-06-13 2013-08-20 Basf Se Process for the production of moldings
EP2597123A1 (fr) 2011-11-23 2013-05-29 Basf Se Liant aqueux pour substrats granuleux et/ou fibreux
US9359518B2 (en) 2011-11-23 2016-06-07 Basf Se Aqueous binder for granular and/or fibrous substrates

Also Published As

Publication number Publication date
AU1292983A (en) 1983-11-24
KR890002931B1 (ko) 1989-08-12
AU539800B2 (en) 1984-10-18
US4504640A (en) 1985-03-12
KR840004128A (ko) 1984-10-06
JPS58201811A (ja) 1983-11-24
EP0095233A3 (en) 1984-03-21
EP0095233B1 (fr) 1986-06-04
CA1233945A (fr) 1988-03-08
DE3363895D1 (en) 1986-07-10
JPH0214364B2 (fr) 1990-04-06

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